Datos del Documento


Por favor, use este identificador para citar o enlazar este documento: https://ria.asturias.es/RIA/handle/123456789/7868
Registro de Metadatos Completo
Campo Dublin Core Valor Idioma
dc.contributor.authorJiménez, Azucena-
dc.contributor.authorPérez-Aguilar, M. Carmen-
dc.contributor.authorCabal, María-Paz-
dc.contributor.authorValdés, Carlos-
dc.date.accessioned2017-04-21T12:14:51Z-
dc.date.available2017-04-21T12:14:51Z-
dc.date.issued2016-02-02-
dc.identifier.urihttps://ria.asturias.es/RIA/handle/123456789/7868-
dc.description.abstract1,3-Diaryl-3-trifluoromethylcyclopropenes and 2-aryl- or 2-alkyl 1,3-diaryl-3-trifluoromethylcyclopropenes are prepared in a very simple way by reaction between 1,1,1-trifluoroacetophenone tosylhydrazones and terminal or internal alkynes respectively in a base promoted process that does not require the presence of any metal catalyst. The essential role of the trifluoromethyl group, which enables the formation of the cyclopropenes instead of the expected pyrazoles has been computationaly investigated,suggesting to the participacion of a free carbene.eng
dc.language.isoengeng
dc.relation.isreferencedbyNo, esta versión no ha sido citadaeng
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/deed.eseng
dc.subjectTosylhydrazoneeng
dc.subjectCyclopropeneeng
dc.titleSynthesis of 1,3-Diaryl-3-trifluoromethylcyclopropenes by Transition-Metal-Free Reaction of 2,2,2-Trifluoroacetophenone Tosylhydrazones with Alkynes: The Effect of the Trifluoromethyl Groupeng
dc.typepreprinteng
Aparece en las colecciones: Open Access DRIVERset
Química

Archivos en este documento:
Fichero Tamaño Formato  
Archivo.pdf697.35 kBAdobe PDFVer/Abrir
Mostrar el registro Básico


Ver estadísticas del documento


Este documento está sujeto a una licencia Creative Commons: Licencia Creative Commons Creative Commons